EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS180-15666 
Organism
Homo sapiens 
Tissue/cell
Small_intestine 
Coordinate
chr14:100044550-100047770 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Klf1MA0493.1chr14:100047542-100047553GGCCACACCCA+6.62
SP2MA0516.2chr14:100046817-100046834AAGGGGGCGGGGATGGG-6.04
ZNF263MA0528.1chr14:100045681-100045702GGAGGAAGAGAAGTGGGGGAG+6.04
ZNF263MA0528.1chr14:100045695-100045716GGGGGAGGGGGGCAGGGAGGC+6.11
ZNF263MA0528.1chr14:100045678-100045699GGTGGAGGAAGAGAAGTGGGG+6.69
ZNF263MA0528.1chr14:100046804-100046825AGGGGAGGGGGGGAAGGGGGC+6.75
ZNF263MA0528.1chr14:100047457-100047478AGAGGAGGAGTGGGAGGGTGA+7.04
ZfxMA0146.2chr14:100046480-100046494CAGGCCTGGCCCCC-6.25
Number of super-enhancer constituents: 28             
IDCoordinateTissue/cell
SE_00922chr14:100044482-100046601Adrenal_Gland
SE_06477chr14:100047173-100049145Brain_Hippocampus_Middle
SE_23140chr14:100040149-100047008Colon_Crypt_1
SE_23140chr14:100047165-100047974Colon_Crypt_1
SE_23807chr14:100044472-100047038Colon_Crypt_2
SE_23807chr14:100047221-100047760Colon_Crypt_2
SE_24879chr14:100044342-100047065Colon_Crypt_3
SE_24879chr14:100047217-100048129Colon_Crypt_3
SE_26586chr14:100036268-100048060Esophagus
SE_27780chr14:100044621-100047720Fetal_Intestine
SE_28740chr14:100044751-100047885Fetal_Intestine_Large
SE_31455chr14:100044168-100048125Gastric
SE_40985chr14:100034161-100047061Left_Ventricle
SE_41558chr14:100034157-100047015LNCaP
SE_41558chr14:100047183-100048847LNCaP
SE_42529chr14:100036484-100047048Lung
SE_47508chr14:100044802-100046802Pancreas
SE_47508chr14:100047193-100047929Pancreas
SE_49276chr14:100037919-100046958Right_Atrium
SE_50321chr14:100044222-100047023Sigmoid_Colon
SE_52517chr14:100044484-100047012Small_Intestine
SE_54552chr14:100023051-100046861Stomach_Smooth_Muscle
SE_54552chr14:100047097-100048205Stomach_Smooth_Muscle
SE_57311chr14:100043817-100047007VACO_400
SE_61471chr14:100013991-100069569Toledo
SE_65289chr14:100044656-100048217Pancreatic_islets
SE_68735chr14:100045019-100046812H9
SE_68735chr14:100047264-100048227H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14100045606100045757
Number: 1             
IDChromosomeStartEnd
GH14I099578chr14100044558100048013
Enhancer Sequence
TACAGCCCAT CCTGTATCCC CCATCGGTGT GTTTGTGTGT GTGTGTGAGT GTACACCTCT 60
CCACGCCCAT ACAGCCCATC CTATATCCCC CATCAGTGTG TGTGTGTGTG TGTGTGTGTG 120
TGTACACATC TCCACACCCA TACAGCCCGT CCTGTATCCC CCATCGGTGT GTTTGTGTGT 180
GTGTGTGAGT GTACACCTCT CCACACCCAT ACAGCCCACA CCTATGTTCC CCGTCATGCA 240
GTAGTTCTTA AATGGTAGTG ATGTGGTTGC TTATTCAGTG TGTGTATGTC AACTCCCATC 300
ACTGTGTGTG TGTGACTGTG CACATGTCTC CACACCCACA TGGCCTGTAC CTATGTCCCC 360
TGTCACTGTG TGTGTGAGCC TCCACAGCCT GCACCCTCCT CTTGGTCATG TTCAATGATT 420
TAAAAGCATC CCTCCCCACT GCTTCTATTT TTGCTTTTGA CCTTTAGTTG AATGCTCACA 480
GCTGCTGGGC CGTTGGCGTG ATGGTGAGTT CATCACGTGT AATCGGGAGA CAGGACAATT 540
TTATTTCCTC TAATACAAGC GCTGCTGCCC CAGCCCCCTT CCAAGACCGG AGCTGGCTTC 600
TCTAAGCGCT TCCCTAGAGT GAGGATGTAA TAATCTGCTG GAAGGCGTGA CCGTGCCGTG 660
GAAGGCTCTA GGTGACAGGT GGATGTGGTC CGTGTCACCC TGCTGGTGTT GACACACTCC 720
CTGCCCCACC TCCATCCACA AGCCCTGCTG GGGCATGGAG GAGGGTGCTC TCTTACCAAC 780
ACTTCGGGCT GAGAACCCAC AGACTCTCTC CATTGCTCAT GAAGCCCCTA CTGCAGGTGA 840
GGAAACTGAG GCACAGAGCC CAAGAGAGGT GCTCAGGTCA CACCATGGAG GCCTGTCTGA 900
CCCAGGTGGC CCTGAGTCCA GAGGTGCTCG CCTGGGTACC CACACAGTCC CCTGGGCTCC 960
TGAGTGCCTT TTCCCCCATG AAATGACGTC AGGGAAACCC CCTGTCCTGG GGCTGAAGTT 1020
CTGCCTCCAG CCTTGGTGCC AAACAAGCCA GAGAAGTGGC GGGGCTGCCC CAACAGGCAC 1080
CGTCCTGGAC GCAGTGTCCC TGTGCACACC TGTGGAACCT GCTCTGCCGG TGGAGGAAGA 1140
GAAGTGGGGG AGGGGGGCAG GGAGGCCCAG TGTGACTCCG AGTCTGCTGT GGGCTCAGAG 1200
ATACTCACAC AGTGAGTGGG ACCTACAGGG GAGCTGGCAG GGGCCTGGGG TTGGGGGCTC 1260
CCCCTATCCT GCCCTCCCAG CCCTGGTCCT TCTGCCCAGA TCCCAGGGCA TGTGTTCCCA 1320
GCTGCCCCAC TGACTGCCTC ACTCCCAACT CTTCCTGGAG CCTTCTCCAG GGCGCAGCCC 1380
CAGACAGCCC AGGCAAGAAA CCCAGAAGGA AGAGGTGGGG CCAGAAAGGT GAGGACTGGA 1440
TTCGGGATTG AGGTGGGGGC TATGGTCAGC TCCCTGGGGG AGGCAGCGGG AGGCAGGGGC 1500
AGGCCTGGGG GAGTCCAGGG CAGCGGGGGA GAGGTCCCCA CATGTCAGCT CCTGCCTGCT 1560
GTCACCTCTC CTGATTCCTT CCCCATCCCA CTCAGGAGTG GGGATGGGGG ATCCCATCTC 1620
ACTAATGAGG AAACTGAGAC ACACACGGTT GTTGGTCGTT AGGCTGTCTA CCAGAGGTCG 1680
CCCAAGGCCA GGCCACCCTG CCCACCCCCG TCTGGCTCAG TCCAAGACTT TGGGAGTCTT 1740
GGCCAGGGTA GGGCATTAAT CACCTCAGCA GCGGACCACC ATGACAAACC CCACATACCC 1800
CACATACCCC GGAGTGAGTC ACATGGGCAG GGCTGGCCCC TTCCTCTTGG TCTCACATTC 1860
CTAAACAGTA GACACCTTCC AGGAATTCGG TCAGCAAAGT GGCTGGAGCT GCTGGGACAG 1920
ACAGCCTGTG CAGGCCTGGC CCCCGGCACA CCCAGAGGAA GGAGAGGCTG GGTGGCTCAG 1980
GTGTGGCCCC GGAGCTCGGC AGGCCCAGCC CCCAGGGACA CAGCCCACGT GCACAGTGGG 2040
TGACAGACCA GCTAAGATAT AGTGCTGTCC TAAGAGCTCA AGGCAGAGAC TGCCATTAAC 2100
ACAGCCCAGC CCAGACAGAA GAGCACACCT CCCAGAGTCA CCGTGAGTGC AGTGGGGGAG 2160
GCAGGAGGGG CTTTTGGACA CTGAGGTAGC TGGAAAAGCA AGCAGAGGGC GGCATCTCAG 2220
CCACAGGCTG GAGACATGAG GGACGTCCCC AGTGAGGGGA GGGGGGGAAG GGGGCGGGGA 2280
TGGGGGGAAC TGGAGGCGGA GAAGACAGCC AGGGAAAGAG GGGAGGTATG AAAACGCCTG 2340
GCTAATGGTG TTAAGGAACT GCCACTCATG GCCGGGCATG GTGGCTCACG TCTGTAATCC 2400
CAGCACTTTG GGAGGCCAAG GTGTGTGGCT CATTTGACGT CAGGAGTTCA AGACCAGCCT 2460
GGCCAACATG GTGAAACCCC ACCTCTGCTA AAATTACAAA AATTAGCTGG GCATGGTGGC 2520
GGGCACCTAT AGTCCCAGTT ACTTGGGAGG CTGAAGCAGG AGAATGGCTT GAACCCGGGA 2580
GGCAGAGGTT GCAGTGAGCC AAGATCGCGC GACTGCACTC TAGCCTGGGT GATAGAGCAA 2640
GACTCCATCT CAAGAAAATT AAAAAGGAAC TGCTGTTCAT CTTCTTCCAG AAGACATGGG 2700
AGAGGAATGT GGCAAAGGCA TCAGAGCCTG ATCACAGAGC ACCTCCAACT TTATTTTCAG 2760
AATCCTGAAC CTGATGCTGA GGGGTCCCCA GAGAGCCAAG TGCAGGGTAG GGGCTGTGTT 2820
TCAGGAAAGA CAGAGTGAGG GCTGGAGGAG ACCATCCTGG AGGCAGGGAG GCCAGCTGGG 2880
AGGCTGGTTC CACGATCGCT GAAGCAAAGA GGAGGAGTGG GAGGGTGAAA CCCCACCATC 2940
AGCACTGGAG AAGGAATGGC AGGTGTGCCC AGTGCCACCC TACCCTGGCA AAGGCCACAC 3000
CCATGCTCAA ACCACTGGGC TCTCCAGGGC AAAGACCTGG GCAAGGCAGG ATGGACAGGG 3060
CCTGGTCAAC CCAGAGCCCC GTGAACAGAC CACCAACTAT GCCACACCAA GCTGGTCAGA 3120
CCCACCAGAT GCTGGACCCC GCCTGCAAAG AACACAGCCC CTGAAGACAA CCGTGGAAGT 3180
TCTATCTTCC AGGACAGAGC TGCCAGGTAG GAGGACAGCG 3220